Manager

Why This Role Matters
The Manager plays a critical role in ensuring pharmaceutical manufacturing processes meet regulatory and quality standards. By overseeing validation activities, investigations, and IPQA operations, the role helps maintain product quality, compliance, and operational efficiency within pharmaceutical production environments.

Job Description
Lupin is hiring a Manager for a full-time on-site position in Goa. The role involves managing cleaning validation, process validation, quality investigations, document management, and IPQA operations to ensure compliance with pharmaceutical manufacturing standards and regulatory requirements.

Key Features of the Role
• Position: Manager
• Company: Lupin Limited
• Location: Goa, India
• Employment Type: Full-Time
• Workplace Type: On-site
• Experience: 12–17 years
• Industry: Pharmaceutical Manufacturing

Responsibilities
• Oversee cleaning validation activities in pharmaceutical manufacturing processes
• Manage process validation to ensure consistent product quality
• Conduct and supervise investigations related to deviations and quality issues
• Maintain and review quality documentation and validation records
• Manage document control and ensure compliance with regulatory requirements
• Supervise IPQA (In-Process Quality Assurance) operations during manufacturing
• Coordinate with cross-functional teams to maintain quality standards
• Ensure compliance with internal quality systems and regulatory guidelines
• Support continuous improvement in manufacturing and quality processes

Required Qualification
• Graduation in Pharmacy
• Graduation in Pharmaceutical Technology

Important Requirements
• 12–17 years of experience in pharmaceutical manufacturing or quality operations
• Experience in cleaning validation and process validation
• Knowledge of investigation handling and document management systems
• Understanding of IPQA operations and pharmaceutical quality standards
• Strong leadership and coordination skills

What We Offer
• Opportunity to work with a global pharmaceutical company
• Exposure to large-scale pharmaceutical manufacturing operations
• Professional growth in quality assurance and validation management
• Collaborative work environment with cross-functional teams

Experience and Skills
• Cleaning validation and process validation management
• Quality investigations and deviation handling
• Document management and regulatory compliance
• In-Process Quality Assurance (IPQA) operations
• Cross-functional coordination and team collaboration
• Strategic planning and operational management

Salary Insights
• Salary details are not specified in the job listing
• Compensation may vary based on experience and company policies

Company Overview
Lupin Limited is a global pharmaceutical company headquartered in Mumbai, India. The company develops and manufactures branded and generic formulations, biotechnology products, and active pharmaceutical ingredients. Lupin operates in over 100 markets worldwide with multiple manufacturing facilities and research centers, focusing on improving patient health outcomes through innovation and quality pharmaceutical products.

FAQs

1. What qualifications are required for this role?
   Candidates must have a degree in Pharmacy or Pharmaceutical Technology.

2. How much experience is required?
   The position requires 12–17 years of experience in pharmaceutical manufacturing or quality operations.

3. What are the main responsibilities in this role?
   The role involves managing cleaning validation, process validation, investigations, document management, and IPQA operations.

4. Where is the job located?
   The job is based in Goa, India.

Application Tips
• Highlight your experience in cleaning validation and process validation
• Mention your expertise in quality investigations and IPQA operations
• Include details of your pharmacy or pharmaceutical technology qualification
• Demonstrate leadership and stakeholder management experience
• Emphasize knowledge of pharmaceutical quality and regulatory compliance